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c-Myc调控lncRNA KCTD13-DT对口腔鳞癌的影响

李文丽 朱友明 何家才

安徽医科大学学报2024,Vol.59Issue(10):1759-1768,10.
安徽医科大学学报2024,Vol.59Issue(10):1759-1768,10.DOI:10.19405/j.cnki.issn1000-1492.2024.10.010

c-Myc调控lncRNA KCTD13-DT对口腔鳞癌的影响

Effects of c-Myc regulation of lncRNA KCTD13-DT on oral squamous carcinoma

李文丽 1朱友明 2何家才2

作者信息

  • 1. 安徽医科大学口腔医学院,安徽医科大学附属口腔医院,合肥 230032
  • 2. 安徽医科大学口腔医学院,安徽医科大学附属口腔医院,合肥 230032||安徽省口腔疾病研究中心实验室,合肥 230032
  • 折叠

摘要

Abstract

Objective To explore the action mechanism of long non-coding RNA(lncRNAs)lncRNA KCTD13-DT in oral squamous cell carcinoma(OSCC)and its potential interaction with transcription factor c-Myc,providing a potential diagnostic and therapeutic target for patients with OSCC.Methods The expression of lncRNA KCTD13-DT in OSCC and paracancerous tissues was detected by qRT-PCR.The effects of c-Myc overexpression and knock-down on human tongue squamous carcinoma cells HN6 and CAL27 were detected by qRT-PCR.Fluorescence in si-tu hybridization(FISH)assessed the localization of lncRNA KCTD13-DT in cells.A dual luciferase reporter gene was used to analyze the role of c-Myc in target binding to the promoter region of lncRNA KCTD13-DT.Stable cell lines with knockdown or overexpression of lncRNA KCTD13-DT were constructed in human OSCC cell lines HN6 and CAL27 by lentiviral infection,and the knockdown and overexpression efficiencies of lncRNA KCTD13-DT were detected by qRT-PCR.Cell proliferation changes were detected by growth curve assay,CCK-8 assay,colony forma-tion assay,and cell migration was detected by scratch assay and Transwell.Results lncRNA KCTD13-DT expres-sion level was reduced in OSCC tissues and OSCC cells(HN6,CAL27),and Western blot verified that after knoc-king down and overexpression of c-Myc in HN6 and CAL27,the qRT-PCR experiments showed that c-Myc nega-tively regulated lncRNA KCTD13-DT,and overexpression of c-Myc significantly down-regulated lncRNA KCTD13-DT;knockdown of c-Myc significantly up-regulated lncRNA KCTD13-DT levels.Dual luciferase reporter gene showed that c-Myc could target lncRNA KCTD13-DT,and c-Myc could be involved in regulating and repressing the transcriptional activity of lncRNA KCTD13-DT.FISH showed that lncRNA KCTD13-DT mainly existed in the nu-cleus.Growth curve assay,CCK-8 assay,cell scratch assay,Transwell,and colony formation assay showed that knockdown of lncRNA KCTD13-DT promoted the growth and proliferation of OSCC cells,and overexpression of ln-cRNA KCTD13-DT significantly inhibited the proliferation and migration of OSCC cells.Conclusion lncRNA KCTD13-DT is negatively regulated by c-Myc.Knockdown of lncRNA KCTD13-DT promotes cell proliferation,while overexpression of it inhibits cell growth.

关键词

长链非编码RNA/c-Myc/口腔鳞癌/细胞增殖/细胞迁移

Key words

long non-coding RNA/c-Myc/oral squamous cell carcinoma/cell proliferation/cell migration

分类

医药卫生

引用本文复制引用

李文丽,朱友明,何家才..c-Myc调控lncRNA KCTD13-DT对口腔鳞癌的影响[J].安徽医科大学学报,2024,59(10):1759-1768,10.

基金项目

国家自然科学基金项目(编号:81771117) (编号:81771117)

安徽省自然科学基金项目(编号:2308085Y23) National Natural Science Foundation of China(No.81771117) (编号:2308085Y23)

Natural Science Foundation of Anhui Province(No.2308085Y23) (No.2308085Y23)

安徽医科大学学报

OA北大核心CSTPCD

1000-1492

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